Insulet Corporation recalls OmniPod Insulin Management Product Demonstration Kit; Model Reference Number: (PDK-ZXP490) Product Usage: The Demons

Recalled November 13, 2013 · FDA recall Z-0166-2014 · Insulet

Hazard

Alcohol Prep Pads contained within the kit are not properly labeled. · FDA Class II

Units

5,050 kits

Sold at

Worldwide Distribution - USA Nationwide and the country of Israel.

Description

Alcohol Prep Pads contained within the kit are not properly labeled.

Product

OmniPod Insulin Management Product Demonstration Kit; Model Reference Number: (PDK-ZXP490) Product Usage: The Demonstration Kit (PDK-ZXP490) is an alternate kit provided to potential patients by healthcare professionals for patients to experience what wearing a Pod may feel like prior to purchase. Each Demonstration Kit includes a UST400 brochure, one Alcohol Pad, and a Pod. The OmniPod Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for the quantitative measurement of glucose in fresh whole capillary blood (in vitro) from the finger. The glucose measurements should not be used for the diagnosis of or screening for diabetes. The PDM glucose meter is intended for single-patient use and should not be shared. Abbott FreeStyle test strips are used with the built-in FreeStyle meter for the quantitative measurement of blood glucose in fresh whole capillary blood from the finger, upper arm and palm. Abbott Freestyle Control Solutions are used to verify that the meter and test-strips are working together properly and that the test is performed correctly.

Manufacturer(s)

Insulet Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →